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MilliporeSigma

C1144

Chlorazol Black

Powder

Synonym(s):

4-Amino-3-[[4′-[(2,4-diaminophenyl)azo][1,1′-biphenyl]-4-yl]azo]-5-hydroxy-6-(phenylazo)-2,7-naphthalenedisulfonic acid disodium salt, Chlorazole Black E, Direct Black 38

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5 G

$45.20

25 G

$167.00

$45.20


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About This Item

Empirical Formula (Hill Notation):
C34H25N9Na2O7S2
CAS Number:
Molecular Weight:
781.73
NACRES:
NA.47
PubChem Substance ID:
UNSPSC Code:
12171500
EC Number:
217-710-3
MDL number:
Colour Index Number:
30235

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Product Name

Chlorazol Black,

InChI key

XRPLBRIHZGVJIC-UVHCWRHYSA-L

InChI

1S/C34H27N9O7S2.2Na/c35-22-10-15-27(26(36)18-22)41-38-24-11-6-19(7-12-24)20-8-13-25(14-9-20)40-42-32-28(51(45,46)47)16-21-17-29(52(48,49)50)33(34(44)30(21)31(32)37)43-39-23-4-2-1-3-5-23;;/h1-18,44H,35-37H2,(H,45,46,47)(H,48,49,50);;/q;2*+1/p-2/b41-38+,42-40+,43-39+;;

SMILES string

[Na+].[Na+].Nc1ccc(\N=N\c2ccc(cc2)-c3ccc(cc3)\N=N\c4c(N)c5c(O)c(\N=N\c6ccccc6)c(cc5cc4S([O-])(=O)=O)S([O-])(=O)=O)c(N)c1

form

powder

composition

Dye content, ≥45% (based on Nitrogen)

color

dark brown to black

solubility

H2O: 1 mg/mL

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

Quality Level

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1 of 4

This Item
N9002379298F7253
color

dark brown to black

color

-

color

-

color

brown-red

form

powder

form

powder

form

powder, crystals or chunks

form

powder

solubility

H2O: 1 mg/mL

solubility

water: 1 mg/mL

solubility

-

solubility

water: 10 mg/mL

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

composition

Dye content, ≥45% (based on Nitrogen)

composition

Dye content, ~50%

composition

-

composition

Dye content, ≥25%

General description

Chlorazol Black has strong affinity for cellulose and chitin. In plant tissues, it helps to differentiate between cellulose and lignin.[1] It also helps in distinguishing fungal bodies from artefacts due to chitin staining.[2] It is also used as an auxiliary stain for chromosomes.[3]

Application

Chlorazol Black has been used to monitor the infection of mycorrhizal Allium porrum in plant roots.[4] It has also been used for the staining of copepods.[5]

pictograms

Health hazardExclamation mark

signalword

Danger

Hazard Classifications

Carc. 1B - Eye Irrit. 2 - Repr. 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P2 (EN 143) respirator cartridges


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Mustafa Işik et al.
Journal of hazardous materials, 114(1-3), 29-39 (2004-10-30)
An Upflow Anaerobic Sludge Blanket Reactor/Continuous Stirred Tank Reactor was used sequentially to decolorize and mineralize C.I. Direct Black 38 azo dye (3200 mg/L) in a synthetic wastewater containing glucose as co-substrate. At the steady state conditions color was effectively
Baran R, et al.
Onychomycosis: The Current Approach to Diagnosis and Therapy (1999)
Cell-wall-bound peroxidase activity in roots of mycorrhizal Allium porrum.
Spanu P and Bonfante-Fasolo P
The New phytologist, 109, 119-124 (1988)
R P Bos et al.
Toxicology, 40(2), 207-213 (1986-08-01)
The role of the rat intestinal flora in the azo reduction of some benzidine-based dyes was studied in vitro and in vivo. The formation of benzidine was measured after anaerobic incubation of direct black 38, direct blue 6 and direct
Jianyong An et al.
The New phytologist, 224(1), 396-408 (2019-05-31)
Plants form a mutualistic symbiosis with arbuscular mycorrhizal (AM) fungi, which facilitates the acquisition of scarce minerals from the soil. In return, the host plants provide sugars and lipids to its fungal partner. However, the mechanism by which the AM

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